Commercial Director Iberia

Crit Interim España; Valencia; Presencial; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical industry is seeking a Senior Project Manager to oversee key projects that ensure compliance with GxP regulations and drive IT solutions. This role involves planning, execution, and management of complex projects, requiring extensive experience in project management and strong leadership skills. The ideal candidate will have a proven track record in cross-functional team management and regulatory compliance within the life sciences sector.

Formación

• Minimum 8+ years of project management experience in the pharmaceutical industry.
• Direct experience managing IT projects with GxP compliance.
• Strong knowledge of GxP guidelines and FDA regulations.

Responsabilidades

• Lead and manage high-priority projects in pharmaceuticals.
• Ensure compliance with GxP, FDA, and other regulations.
• Collaborate with stakeholders and manage project risks.

Conocimientos

Leadership

Communication

Stakeholder Management

Problem Solving

Risk Management

Educación

Bachelor’s degree in Pharmaceutical Sciences, Life Sciences, Computer Science, Engineering

PMP, PMI-ACP or similar certifications

Herramientas

MS Project

Jira

Asana

MS Office Suite

Descripción del empleo

We are seeking a Senior Project Manager with extensive experience in the pharmaceutical industry, specifically in managing projects that involve Good Manufacturing Practices (GxP) compliance and IT systems. The ideal candidate will have a proven track record of leading cross-functional teams, driving the delivery of complex projects within the pharmaceutical and life sciences sector, and ensuring compliance with industry regulations. This role is integral to the planning, execution, and management of key projects within a regulated environment, with a focus on integrating IT solutions in support of GxP processes.

Key Responsibilities :

• Project Planning & Execution : Lead and manage multiple high-priority projects, ensuring adherence to project timelines, scope, budget, and quality standards. Coordinate project resources and deliverables to meet business objectives.
• Regulatory & GxP Compliance : Ensure all projects are delivered in strict accordance with GxP, FDA, and other applicable regulatory requirements. Oversee the implementation of IT systems and solutions within the pharmaceutical environment, ensuring that they meet industry standards.
• Stakeholder Management : Collaborate with internal and external stakeholders, including business leaders, regulatory bodies, and IT teams. Maintain clear communication to manage expectations, mitigate risks, and resolve issues as they arise.
• Risk Management : Proactively identify and address risks associated with project delivery, including those related to regulatory compliance, resource allocation, and IT systems integration. Develop and implement mitigation strategies.
• IT System Integration : Manage the end-to-end lifecycle of IT-related projects, from requirement gathering to system design, implementation, and post-deployment support. Ensure that IT solutions are aligned with GxP and other regulatory guidelines.
• Team Leadership & Development : Lead cross-functional teams, including project managers, IT professionals, regulatory experts, and business analysts. Provide mentorship and guidance to junior project managers and team members.
• Continuous Improvement : Drive process improvements within the project management function, adopting best practices and methodologies (e.g., Agile, Waterfall) to increase efficiency, effectiveness, and compliance in project delivery.

Qualifications :

• Education : Bachelor’s degree in Pharmaceutical Sciences, Life Sciences, Computer Science, Engineering, or related field. PMP, PMI-ACP, or similar certifications are a plus.
• Experience : Minimum 8+ years of project management experience in the pharmaceutical industry with direct experience in managing IT projects that involve GxP compliance. Proven experience in leading large-scale, cross-functional IT initiatives in regulated environments (e.g., pharmaceutical manufacturing, clinical trials, or laboratory environments). Strong knowledge and understanding of GxP guidelines, FDA regulations, and the impact on pharmaceutical IT systems. Experience with pharmaceutical IT infrastructure, including but not limited to LIMS, ERP, MES, and validated systems.
• Skills & Competencies : Strong leadership and team management skills. Excellent communication and stakeholder management abilities. Ability to navigate complex regulatory environments. Strong problem-solving and risk management skills. Proficiency in project management software (e.g., MS Project, Jira, Asana) and MS Office Suite. Ability to prioritize and manage multiple projects simultaneously.

Preferred Qualifications :

• Experience with ERP, LIMS, or other pharmaceutical IT systems.
• Expertise in Agile methodologies and project management techniques.
• Advanced degree in Life Sciences or related field.

J-18808-Ljbffr